A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026007



Internal ID20593047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59870992..59871980hg38UCSC Ensembl
chr15:60163191..60164179hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38989
hg19989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer